Fluid Venting Activity on the Costa Rica Margin: New Results from Authigenic Carbonates

Carbonate precipitates on mounds and along tectonic scarps off the Costa Rica margin are manifestations of subduction-induced dewatering. The long-term dewatering history is recorded in mineralogical, petrological and isotope signals of carbonates recovered from these sites. The carbonates are strongly depleted in δ13C (−11 to −53‰ PDB) and enriched in δ18O (+4 to +8‰ PDB). Thermogenic methane and biogenic methane were identified as sources of the carbon. Chemoherm carbonates and seepage-associated carbonates formed in a focused flow regime have lighter δ13C values, while others formed in a more diffusive flow regime have slightly enriched C isotope values. Three fluid components were inferred based on the calculation of equilibrium δ18O: clay dehydration water, gas hydrate water and seawater. Calculated equilibrium δ18O values of carbonates from different down-core depths as well as from different precipitation stages show that the δ18O of the precipitating fluid is progressively depleted with time. Dolostones showing a methane-C source and a well constrained O-isotope signature are thought to have formed at depth in the sediment and subsequently became exhumed. Glauconitic sandstones cemented by methane-derived carbonate provide evidence that fluid and solid material have been expelled by the mud volcano

Numerical simulation of two coalescing turbulent forced plumes in linearly stratified fluids.

Author Posting. © AIP Publishing, 2019. This article is posted here by permission of [publisher] for personal use, not for redistribution. The definitive version was published in Lou, Y., He, Z., Jiang, H., & Han, X. Numerical simulation of two coalescing turbulent forced plumes in linearly stratified fluids. Physics of Fluids, 31(3), (2019):037111, doi:10.1063/1.5087534.A computational fluid dynamic model that can solve the Reynolds-averaged Navier-Stokes equations and the species transport equation is developed to simulate two coalescing turbulent forced plumes, which are released with initial momentum and buoyancy flux into a linearly stable stratified environment. The velocity fields, turbulence structures, and entrainment of two plumes with different source separations and source buoyancy fluxes are analyzed quantitatively, in comparison with a series of physical experiments. An empirical parameterization is proposed to predict the amplification of the maximum rise height of two coalescing forced plumes caused by superposition and mutual entrainment. The maximum values of both turbulent kinetic energy and turbulence dissipation rate decrease monotonically with the increase in source separation of the two turbulent plumes. However, the trajectory of the maximum turbulent viscosity attained in the plume cap region presents two notable enhancements. This variation may be attributed to the turbulence transported from the touching region and the strong mixing around the neutrally buoyant layer between two plumes, while the mixing is caused by the lateral convection and the rebound after overshooting. The plume entrainment coefficient in near vent stems has a positive relationship with the source Richardson number. A transition of flow regimes to plume-like flows would occur when the contribution of initial momentum is important. The entrainment coefficient will decrease in the touching region of two plumes due to mutual entrainment, while the superposition of plumes can lead to distortion of the boundary of plume sectors.This work was financially supported by the National Natural Science Foundation of China (Grant No. 11672267) and Fundamental Research Funds for the Central Universities (Grant No. 2017XZZX001-02A). This work was supported by HPC Center of ZJU (Zhoushan campus). Yingzhong Lou would like to thank Liang Zhao at Zhejiang University for fruitful discussions. The authors gratefully acknowledge the constructive suggestions offered by the anonymous referees.2020-03-2

Spatial and temporal evolution and driving factors of county solid waste harmless disposal capacity in China

Currently, China mainly adopts the waste treatment model of “household sorting, village collection, town transfer and county disposal.” Determining the spatial and temporal distribution of China’s county solid waste harmless disposal capacity and formulating strategies according to local conditions are of great significance in promoting the construction of beautiful villages in China and realizing the Beautiful China strategy. This paper explores the spatial and temporal evolution characteristics of county solid waste harmless disposal capacity by selecting relevant data from 27 provinces in China from 2006 to 2020, and adopts the Dagum Gini coefficient method to measure the spatial gap of it. In addition, this paper empirically analyses the drivers affecting county solid waste harmless disposal capacity using the spatial Durbin model (SDM). The main conclusions are as follows: 1) In terms of time, county solid waste harmless disposal capacity in China as a whole shows a year-by-year increasing trend, especially after 2018 when the growth rate is faster. 2) In terms of spatial patterns, the solid waste harmless disposal capacity of coastal areas is generally higher than that of inland areas, and the distribution of provinces with low and middle levels of solid waste harmless disposal capacity is characterized by concentrated contiguity. From the perspective of spatial agglomeration, the characteristics of spatial agglomeration in the north are gradually becoming more pronounced, while those in the south are not significant. From the trajectory of the evolution of the spatial center of gravity, the center of gravity of county solid waste harmless disposal capacity as a whole shows a northeast, then northwest, then northeast movement, and the speed of “northward expansion” is greater than the speed of “eastward expansion”. 3) The results of the Dagum Gini coefficient and its decomposition show that the northeast has the smallest average annual rate of change in the Gini coefficient. The reduction of the within-group gap is an important driver towards equilibrium. The contribution of hypervariable density is decreasing year by year. 4) The number of harmless disposal plants, GDP per person, population urbanization, the number of township waste transfer stations and county waste disposal fixed asset investment are important drivers of county waste harmless disposal capacity. Findings provide helpful insights into optimizing rural habitat and promoting the comprehensive transformation of China’s county development

Trace Metal Distribution in Sulfide Minerals from Ultramafic-Hosted Hydrothermal Systems: Examples from the Kairei Vent Field, Central Indian Ridge

The ultramafic-hosted Kairei vent field is located at 25°19′ S, 70°02′ E, towards the Northern end of segment 1 of the Central Indian Ridge (CIR-S1) at a water depth of ~2450 m. This study aims to investigate the distribution of trace elements among sulfide minerals of differing textures and to examine the possible factors controlling the trace element distribution in those minerals using LA-ICP-MS spot and line scan analyses. Our results show that there are distinct systematic differences in trace element distributions throughout the different minerals, as follows: (1) pyrite is divided into three types at Kairei, including early-stage euhedral pyrite (py-I), sub-euhedral pyrite (py-II), and colloform pyrite (py-III). Pyrite is generally enriched with Mo, Au, As, Tl, Mn, and U. Pyrite-I has high contents of Se, Te, Bi, and Ni when compared to the other types; py-II is enriched in Au relative to py-I and py-III, but poor in Ni; py-III is enriched in Mo, Pb, and U but is poor in Se, Te, Bi, and Au relative to py-I and py-II. Variations in the concentrations of Se, Te, and Bi in pyrite are most likely governed by the strong temperature gradient. There is generally a lower concentration of nickel than Co in pyrite, indicating that our samples precipitated at high temperatures, whereas the extreme Co enrichment is likely from a magmatic heat source combined with an influence of serpentinization reactions. (2) Chalcopyrite is characterized by high concentrations of Co, Se, and Te. The abundance of Se and Te in chalcopyrite over the other minerals is interpreted to have been caused by the high solubilities of Se and Te in the chalcopyrite lattice at high temperatures. The concentrations of Sb, As, and Au are relatively low in chalcopyrite from the Kairei vent field. (3) Sphalerite from Zn-rich chimneys is characterized by high concentrations of Sn, Co, Ga, Ge, Ag, Pb, Sb, As, and Cd, but is depleted in Se, Te, Bi, Mo, Au, Ni, Tl, Mn, Ba, V, and U in comparison with the other minerals. The high concentrations of Cd and Co are likely caused by the substitution of Cd2+ and Co2+ for Zn2+ in sphalerite. A high concentration of Pb accompanied by a high Ag concentration in sphalerite indicates that Ag occurs as Pb–Ag sulfosalts. Gold is generally low in sphalerite and strongly correlates with Pb, suggesting its presence in microinclusions of galena. The strong correlation of As with Ge in sphalerite from Kairei suggests that they might precipitate at medium temperatures and under moderately reduced conditions. (4) Bornite–digenite has very low concentrations of most trace elements, except for Co, Se, and Bi. Serpentinization in ultramafic-hosted hydrothermal systems might play an important role in Au enrichment in pyrite with low As contents. Compared to felsic-hosted seafloor massive sulfide deposits, sulfide minerals from ultramafic-hosted deposits show higher concentrations of Se and Te, but lower As, Sb, and Au concentrations, the latter often attributed to the contribution of magmatic volatiles. As with typical ultramafic-hosted seafloor massive sulfide deposits, Se enrichment in chalcopyrite from Kairei indicates that the primary factor that controls the Se enrichment is temperature-controlled mobility in vent fluids

Mineralogical and geochemical features of sulfide chimneys from the 49°39′E hydrothermal field on the Southwest Indian Ridge and their geological inferences

© The Author(s), 2011. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Chinese Science Bulletin 56 (2011): 2828-2838, doi:10.1007/s11434-011-4619-4.During January–May in 2007, the Chinese research cruise DY115-19 discovered an active hydrothermal field at 49°39′E/37°47′S on the ultraslow spreading Southwest Indian Ridge (SWIR). This was also the first active hydrothermal field found along an ultraslow-spreading ridge. We analyzed mineralogical, textural and geochemical compositions of the sulfide chimneys obtained from the 49°39′E field. Chimney samples show a concentric mineral zone around the fluid channel. The mineral assemblages of the interiors consist mainly of chalcopyrite, with pyrite and sphalerite as minor constitunets. In the intermediate portion, pyrite becomes the dominant mineral, with chalcopyrite and sphalerite as minor constitunets. For the outer wall, the majority of minerals are pyrite and sphalerite, with few chalcopyrite. Towards the outer margin of the chimney wall, the mineral grains become small and irregular in shape gradually, while minerals within interstices are abundant. These features are similar to those chimney edifices found on the East Pacific Rise and Mid-Atlantic Ridge. The average contents of Cu, Fe and Zn in our chimney samples were 2.83 wt%, 45.6 wt% and 3.28 wt%, respectively. The average Au and Ag contents were up to 2.0 ppm and 70.2 ppm respectively, higher than the massive sulfides from most hydrothermal fields along mid-ocean ridge. The rare earth elements geochemistry of the sulfide chimneys show a pattern distinctive from the sulfides recovered from typical hydrothermal fields along sediment-starved mid-ocean ridge, with the enrichment of light rare earth elements but the weak, mostly negative, Eu anomaly. This is attributed to the distinct mineralization environment or fluid compositions in this area.This work was supported by the China Ocean Mineral Resources Research and Development Association Program (DY115- 02-1-01) and the State Oceanic Administration Youth Science Fund (2010318)

Tephra records from abyssal sediments off western Sumatra in recent 135 ka: evidence from Core IR-GC1

Three volcanic ash layers were identified in a deep-sea Core IR-GC1 from the north-eastern Indian Ocean, adjacent to western Indonesian arc. They were dominated by glass shards with minor mineral crystals, such as plagioclase, biotite, and hornblende. According to the morphology and major element compositions of the representative glass shards, combined with the 18O-based age, it is suggested that ash Layer A is correlated to the youngest Toba tuff (YTT), Layer B is supposed to be associated with a new eruption of Toba caldera in an age of 98 to 100 ka. Ash Layer C is different the geochemistry characteristics than those of Layer A and Layer B, suggesting that Layer C was not originated from Toba but registered another volcanic eruption event

Past methane release events and environmental conditions at the upper continental slope of the South China Sea: constraints by seep carbonates

Authigenic carbonates and seep biota are archives of seepage history and record paleo-environmental conditions at seep sites. We obtained the timing of past methane release events at the northeastern slope of the South China Sea based on U/Th dating of seep carbonates and seep bivalve fragments from three sites located at 22°02′–22°09′N, 118°43′–118°52′E (water depths from 473 to 785 m). Also, we were able to reconstruct the paleo-bottom water temperatures by calculating the equilibrium temperature using the ages, the corresponding past δ18O of seawater (δ18Osw) and the δ18O of the selected samples formed in contact with bottom seawater with negligible deep fluid influence. A criterion consists of mineralogy, redox-sensitive trace elements and U/Th-isotope systematics is proposed to identify whether the samples were formed from pore water or have been influenced by deep fluid. Our results show that all methane release events occurred between 11.5 ± 0.2 and 144.5 ± 12.7 ka, when sea level was about 62–104 m lower than today. Enhanced methane release during low sea-level stands seems to be modulated by reduced hydrostatic pressure, increased incision of canyons and increased sediment loads. The calculated past bottom water temperature at one site (Site 3; water depth: 767–771 m) during low sea-level stands 11.5 and 65 ka ago ranges from 3.3 to 4.0 °C, i.e., 1.3 to 2.2 °C colder than at present. The reliability of δ18O of seep carbonates and bivalve shells as a proxy for bottom water temperatures is critically assessed in light of 18O-enriched fluids that might be emitted from gas hydrate and/or clay dehydration. Our approach provides for the first time an independent estimate of past bottom water temperatures of the upper continental slope of the South China Sea

Geochemical Investigations of Fe-Si-Mn Oxyhydroxides Deposits in Wocan Hydrothermal Field on the Slow-Spreading Carlsberg Ridge, Indian Ocean: Constraints on Their Types and Origin

We have studied morphology, mineralogy and geochemical characteristics of Fe-oxyhydroxide deposits from metal-enriched sediments of the active (Wocan-1) and inactive (Wocan-2) hydrothermal sites (Carlsberg Ridge, Northwest Indian Ocean). Fe-oxyhydroxide deposits on the Wocan-1 site are reddish-brownish, amorphous and subangular. They occur in association with sulfides (e.g., pyrite, chalcopyrite and sphalerite) and sulfate minerals (e.g., gypsum and barite). The geochemical composition shows enrichment in transition metals (Ʃ (Cu + Co + Zn + Ni) = ~1.19 wt. %) and low (<0.4 wt. %) values of Al/(Al + Fe + Mn) ratio. The Wocan-2 samples show poorly crystallized reddish brown and yellowish Fe-oxyhydroxide, with minor peaks of goethite and manganese oxide minerals. The mineral assemblage includes sulfide and sulfate phases. The geochemical compositions show two distinct types (type-1 and type-2). The type-1 Fe-oxyhydroxides are enriched in transition metals (up to ~1.23 wt. %), with low values of Fe/Ti vs. Al/(Al + Fe + Mn) ratio similar to the Wocan-1 Fe-oxyhydroxides. The type-2 Fe-oxyhydroxides are depleted in transition metals, with Al/(Al + Fe + Mn) ratio of 0.003–0.58 (mean value, 0.04). The ridge flank oxyhydroxides exhibit an extremely low (mean value ~ 0.01) Fe/Mn ratio and a depleted concentration of transition metals. Our results revealed that the Wocan-1 Fe-oxyhydroxides and type-1 Fe-oxyhydroxides of the Wocan-2 site are in the range of Fe-oxyhydroxides deposits that are precipitated by mass wasting and corrosion of pre-existing sulfides. The type-2 Fe-oxyhydroxides are precipitated from sulfide alteration by seawater in an oxygenated environment relative to type-1. The association of biogenic detritus with the oxyhydroxides of the ridge flanks and the low Fe/Mn ratio suggests hydrogenous/biogenic processes of formation and masked hydrothermal signatures with distance away from the Wocan hydrothermal field

Mineralogy and geochemistry of hydrothermal precipitates from Kairei hydrothermal field, Central Indian Ridge

The Kairei hydrothermal field was the first confirmed active submarine hydrothermal system on the Central Indian Ridge. It has been suggested to be related to mafic as well as ultramafic host rocks based on vent fluid composition and the presence of ultramafic rocks in its vicinity. In this study, detailed geochemical and mineralogical analyses have been carried out on the hydrothermal precipitates from the Kairei vent field in order to investigate the possible presence of indications for an ultramafic substrate at this vent site. The studied samples included fragments of sulfide chimneys, massive sulfides and talc-bearing and silicified breccias. Three mineralization stages were identified: (1) a high-temperature stage consisting largely of chalcopyrite, isocubanite, and pyrite; (2) a medium to low temperature stage characterized by the mineral assemblages of sphalerite and pyrite; and (3) a weathering stage characterized by secondary Cu-sulfides (bornite, digenite, covellite and idaite), Fe-oxihydroxides, Opal-A, and Cu-chloride (paratacamite and atacamite). The sulfide geochemistry is characterized by high concentrations of Cu and Zn (Cu + Zn up to 29.3 wt.%, n = 17) and Au (mean 5.28 ppm, n = 17), which is comparable to results from seafloor massive sulfides collected from ultramafic-hosted sites in the Atlantic Ocean, but differs from those of typical mafic-hosted deposits. The high concentrations of Cu and Au at the Kairei hydrothermal field could be an indication for the involvement of ultramafic rocks in the subseafloor. Ultramafic-hosted, Au-rich sulfide deposits may not be restricted to the Atlantic Ocean and may be common along all slow- and intermediate-spreading ridges